chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34169102541691026GT20GENIChomozygous148220358
34169288741692888GA14GENIChomozygous147659188
34169499641694997CT24GENIChomozygous148220359
34169583441695835TC5GENIChomozygous143881115
34169678741696788CA25GENIChomozygous148220360
34169712441697125CT14GENIChomozygous148220361
34169861641698617TC33GENIChomozygous147659192
34169943041699431CT24GENIChomozygous148220362
34169992941699930GA25GENIChomozygous147659193
34170052041700521TC17GENIChomozygous147659194
34170207241702073CT22GENIChomozygous148220363
34170377441703777GAG25GENIChomozygous148219183
34170045341700454T9GENICpossibly homozygous147654563
34170148741701488T17GENIChomozygous147654564
34170205541702056T22GENIChomozygous143854876
34170468941704690CT29GENIChomozygous147659197
34170548841705489CA28GENIChomozygous147659198
34170558841705589CT27GENIChomozygous148220364
34170565641705657AG29GENIChomozygous147659199
34170681441706815AG15GENIChomozygous143881123